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1 CML28 was used to generate a CML28-specific murine monoclonal antibody.
2 cytometry using FITC-conjugated anti-rat IgM murine monoclonal antibody.
3 ine pancreas was used to generate a panel of murine monoclonal antibodies.
4 y after single administration was lower than murine monoclonal antibodies.
5 es have been defined and characterized using murine monoclonal antibodies.
6 ified enzyme was used to generate a panel of murine monoclonal antibodies.
7 ously defined epitopes for broadly conserved murine monoclonal antibodies.
8 ked immunosorbent assay using group-specific murine monoclonal antibodies.
9 ) and light (L) chains were determined for a murine monoclonal antibody, 12/231/93, which is specific
12 in an orthotopic murine xenograft using the murine monoclonal antibody 17.1A conjugated to the photo
15 c efficacy of astatine-211 ((211)At)-labeled murine monoclonal antibody 7G7/B6 alone and in combinati
16 that reduced binding and neutralization by a murine monoclonal antibody (A20) were localized, while m
18 al growth factor receptor chimeric human and murine monoclonal antibody, administered with cisplatin
19 celiac-toxic epitopes was measured by using murine monoclonal antibodies against gliadin and high-mo
22 ecular rationale for the inability to obtain murine monoclonal antibodies against the receptor bindin
23 chemotaxis of human VSMCs that is blocked by murine monoclonal antibody against CCR8 and by the G-pro
24 nal anti-CCR8 antibody and a newly developed murine monoclonal antibody against CCR8 inhibited this a
25 man macrophages using virions opsonized by a murine monoclonal antibody against the MV hemagglutinin
26 the immune response, which develops against murine monoclonal antibodies, allowing for multiple dose
29 finity-purified immunoglobulin fractions and murine monoclonal antibodies and show that antibodies to
32 Fv antibody fragments from the CD20-specific murine monoclonal antibody B9E9 were genetically enginee
34 the present study we have identified a novel murine monoclonal antibody, BOB93, which bound to the su
35 (90)Y-ibritumomab tiuxetan consists of a murine monoclonal antibody covalently attached to a meta
37 e further characterized the targeting of the murine monoclonal antibody DAB4 specifically to dead tum
41 assigned to receive 2 doses of either E5, a murine monoclonal antibody directed against endotoxin (n
42 been most widely used clinically is OKT3, a murine monoclonal antibody directed against the CD3 rece
43 uzumab (HuM195) is an unconjugated humanized murine monoclonal antibody directed against the cell sur
45 ignificant limitation to the repeated use of murine monoclonal antibodies for treatment of transplant
49 e characterization of a broadly neutralizing murine monoclonal antibody, H5M9, to most H5N1 clades an
52 e number of isolates that did not react with murine monoclonal antibodies indicates that DNA sequence
53 neutralizing epitopes on gD2 are targeted by murine monoclonal antibodies, it is not known whether th
54 man platelet factor 4 (PF4)/heparin-specific murine monoclonal antibody (KKO) binds to peripheral blo
57 ation of each of the 3 human FcgammaR, using murine monoclonal antibodies (mAb) to each receptor as a
59 rmined the affinities of two cocaine-binding murine monoclonal antibodies (mAb: clones 3P1A6 and MM02
63 (1), IgG(2a), and IgG(2b) switch variants of murine monoclonal antibody (mAb) 3E5 IgG(3) with identic
64 ducreyi 35000 defective in expression of the murine monoclonal antibody (MAb) 3F11 epitope on H. ducr
67 y, the use of a radiolabeled fibril-reactive murine monoclonal antibody (mAb) as an amyloid-specific
68 imicrotubule agent, covalently linked to the murine monoclonal antibody (mAb) B-B4 targeting syndecan
69 We investigated the functional activity of murine monoclonal antibody (MAb) B5 that recognizes a hi
70 igated the antigenic targets of a protective murine monoclonal antibody (MAb) prepared against a N-Pr
72 III coat protein of fd phage using C355.1, a murine monoclonal antibody (mAb) that recognizes a confo
74 To circumvent this problem, we developed a murine monoclonal antibody (mAb) to human (h) PF4/hepari
77 study tested the hypothesis that a humanized murine monoclonal antibody (MAb) would protect against R
81 Here, we identify a panel of 18 neutralizing murine monoclonal antibodies (mAbs) against the EEEV E2
84 d evaluated for the effects of GPVI-specific murine monoclonal antibodies (mAbs) on platelet survival
86 apeutic doses of 131I-labeled NP-4 and MN-14 murine monoclonal antibodies (MAbs) reactive with carcin
92 ) to determine the reactivity patterns of 21 murine monoclonal antibodies (MAbs) with structurally de
94 e generated and subsequently characterized 7 murine monoclonal antibodies (MAbs), which fell into 4 d
95 ressed this question using quinine-dependent murine monoclonal antibodies (mAbs), which, in vitro and
101 s evaluated with a group of affinity-diverse murine monoclonal antibodies (MoAbs) specific for human
104 sted the hypothesis that the CA-125-specific murine monoclonal antibody, oregovomab, administered as
106 [Chemical reaction: See text] 29G12 is a murine monoclonal antibody programmed to catalyze the re
109 ts with adenocarcinomas reactive to NR-LU-10 murine monoclonal antibody received the 3 components.
112 ue immunoassays with human IgE antibodies or murine monoclonal antibodies showed that these allergens
113 Here we report the development of novel murine monoclonal antibodies specific for different G4 D
119 avy- and light-chain variable regions from a murine monoclonal antibody that recognize Pseudomonas ae
121 ilized Fv fragment (dsFv) was derived from a murine monoclonal antibody that recognizes the alpha sub
122 ensitive), each conjugated with mAb H18/7, a murine monoclonal antibody that recognizes the extracell
125 adult bone marrow mononuclear cells using a murine monoclonal antibody to human platelet glycoprotei
127 (Id)-bearing antibodies sharing an Id with a murine monoclonal antibody to myelin basic protein pepti
130 fragments of CB2, an immunoglobulin G1kappa murine monoclonal antibody, to an epitope in the carboxy
132 sis, we treated human endothelial cells with murine monoclonal antibody W6/32 to HLA class I and then
137 22 different serovar-specific or bispecific murine monoclonal antibodies were localized with synthet
140 thymectomized and treated with Ox8 and Ox38 murine monoclonal antibodies, which deplete CD8+ and CD4
141 d hybridoma technology for the generation of murine monoclonal antibodies with predetermined antigen-